Canonical Allele Identifier: CA2633778498
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67435448-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435448G>A , CM000678.2:g.67435448G>A GRCh38
NC_000016.9:g.67469351G>A , CM000678.1:g.67469351G>A GRCh37
NC_000016.8:g.66026852G>A NCBI36
NG_016549.1:g.9316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.266-180G>A MANE Select ENSP00000316786.5:n.266-180G>A
ENST00000326152.5:c.266-180G>A ENSP00000316786.5:n.266-180G>A
ENST00000566606.1:c.149-85G>A ENSP00000473429.1:n.149-85G>A
ENST00000567684.2:n.129-180G>A
NM_000196.3:c.266-180G>A NP_000187.3:n.266-180G>A
NM_000196.4:c.266-180G>A MANE Select NP_000187.3:n.266-180G>A
Search 100 bp 5'
Search 100 bp 3'